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Janel O Johnson

Showing results (1-10 of 27) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|November 3, 2006
Smoking-responsive juvenile-onset ParkinsonismHasmet Ayhan Hanagasi, Andrew Lees, Janel O Johnson, et al.
Muscle & Nerve|January 1, 2017
Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathyJames B Caress, Janel O Johnson, Yevgeniya A Abramzon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2005
Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 yearsNaheed L Khan, Wagner Horta, Louise Eunson, et al.
Neurobiology of Aging|May 11, 2012
Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosisYevgeniya Abramzon, Janel O Johnson, Sonja W Scholz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndromeJanel O Johnson, Giovanni Stevanin, Joyce van de Leemput, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Brain : a Journal of Neurology|June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron diseaseJanel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
Neurology|June 30, 2012
A candidate gene for autoimmune myasthenia gravisGuida Landouré, Melanie A Knight, Horia Stanescu, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2010
Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patientsBryan J Traynor, Michael Nalls, Shiao-Lin Lai, et al.
Neurobiology of Aging|January 18, 2015
Small deletion in C9orf72 hides a proportion of expansion carriers in FTLDSara Rollinson, Janis Bennion Callister, Kate Young, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Movement Disorders : Official Journal of the Movement Disorder Society|November 3, 2006
Smoking-responsive juvenile-onset ParkinsonismHasmet Ayhan Hanagasi, Andrew Lees, Janel O Johnson, et al.
Muscle & Nerve|January 1, 2017
Exome sequencing establishes a gelsolin mutation as the cause of inherited bulbar-onset neuropathyJames B Caress, Janel O Johnson, Yevgeniya A Abramzon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 11, 2005
Parkin disease in a Brazilian kindred: Manifesting heterozygotes and clinical follow-up over 10 yearsNaheed L Khan, Wagner Horta, Louise Eunson, et al.
Neurobiology of Aging|May 11, 2012
Valosin-containing protein (VCP) mutations in sporadic amyotrophic lateral sclerosisYevgeniya Abramzon, Janel O Johnson, Sonja W Scholz, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 30, 2014
A 7.5-Mb duplication at chromosome 11q21-11q22.3 is associated with a novel spastic ataxia syndromeJanel O Johnson, Giovanni Stevanin, Joyce van de Leemput, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Brain : a Journal of Neurology|June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron diseaseJanel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
Neurology|June 30, 2012
A candidate gene for autoimmune myasthenia gravisGuida Landouré, Melanie A Knight, Horia Stanescu, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 23, 2010
Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patientsBryan J Traynor, Michael Nalls, Shiao-Lin Lai, et al.
Neurobiology of Aging|January 18, 2015
Small deletion in C9orf72 hides a proportion of expansion carriers in FTLDSara Rollinson, Janis Bennion Callister, Kate Young, et al.
Pageof 3